Philips Consumer Lifestyle B.V. is one of 138 FDA 510(k) medical device manufacturers from Netherlands in the dataset, ranked by real submission volume.
Philips Consumer Lifestyle B.V. - FDA 510(k) Cleared Devices
Recent clearances: Philips Avent Natural Care Hands-free Wearable Electric Breast Pump (Model: SCF593/52, SCF593/62), Philips Lumea IPL, Philips Lumea IPL
3
Total
3
Cleared
0
Denied
Philips Consumer Lifestyle B.V. has 3 FDA 510(k) cleared medical devices. Based in Drachten, NL.
Latest FDA clearance: Sep 2026. Active since 2025. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Philips Consumer Lifestyle B.V. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Philips Personal Health, Philips North America, LLC, Philips Personal Health, a subsidiary of Philips North America, LLC and Philips Personal Health, A Subsidiary of Philips.
FDA 510(k) Regulatory Record - Philips Consumer Lifestyle B.V.
3 devices